A strong emphasis has recently been put on mental health practitioners incorporating evidence in their clinical decision-making [Reference Whaley and Davis1, Reference Eibling, Fried, Blitzer and Postma2]. However, this process is challenged by practitioners’ limited resources to keep up to date with advances in research and the complex presentations of mental health issues encountered in clinical practice. Severe behavioural problems (SBPs) in children could be particularly challenging in this respect, as their clinical manifestation varies drastically between individuals. Consequently, over the years, clinical practice guidelines for diagnosing and treating SBPs in children have been developed in several European countries . The scope of these guidelines is to support practitioners in taking evidence-based clinical decisions to maximise the effectiveness of treatment allocation and treatment outcomes [Reference Francke, Smit, de Veer and Mistiaen4]. Yet, a summary of the prevalence and views of these clinical guidelines for SBPs in children around Europe is missing. Developing such a European knowledge base could stimulate national and international collaboration within mental health services and across multi-disciplinary services, which often provide care to children with SBPs [Reference Koivusalo, Labonte, Wibulpolprasert, Kancahanchitra, Leppo, Ollila, Pena, Wismar and Cook5]. Additionally, a European knowledge base provides insight into which elements facilitate the implementation of guidelines and how guidelines could be better tailored to clinical practice. Consequently, this paper aimed to offer a first insight on the availability, perceived value and critical needs of clinical guidelines for SBPs in children across Europe, according to academic experts’ perceptions.
SBPs in children are highly prevalent [Reference Matthys6] and predict negative costly outcomes later in life [Reference Dodge, Coie, Lynam, Eisenberg, Damon and Lerner7, Reference Quy and Stringaris8]. Moreover, they are associated with alarming rates of poor response to or dropout from treatment [Reference Lahey and Waldman9, Reference Chacko, Jensen, Lowry, Cornwell, Chimklis and Chan10]. SBPs in children can be described within the framework of diagnostic categories such as Oppositional Defiant Disorder (ODD) and Conduct Disorder (CD) [11, Reference World Health Organization12]. However, their conceptualisation varies across Europe, as does the diagnostic classification system used [Reference Goodman, Scott S. Child and Adolescent Psychiatry13]. Moreover, there has been an increasing drive in transitioning from categorical diagnoses towards a more dimensional bio-psycho-social case formulation [Reference Johnstone14, Reference Vanheule15]. To allow for a degree of applicability to each country’s national standards, policies and conceptualization of behavioural problems, whilst still preserving uniformity in guidelines referred to, using the broader SBPs term was deemed appropriate. Hence, SBPs in childhood (6–12 years old) were defined as persistent, frequent, and impairing oppositional, defiant, and aggressive behaviours, occurring across several settings, and placed at the severe end of the behavioural disorders spectrum [Reference Matthys6, Reference Dodge, Coie, Lynam, Eisenberg, Damon and Lerner7, Reference Carr16]. The term is virtually equivalent with previously used umbrella terms such as ‘disruptive behaviour disorders/ problems’ [e.g., Reference Smith, Koerting, Latter, Knowles, Mccann and Thompson17–19].
Efforts to improve clinical practices for SBPs in children were marked by the development of official clinical guidelines on SBPs in several European countries. According to the Institute of Medicine , these guidelines were created based on recent systematic reviews and comprise of empirically-supported strategies for assessing and treating SBPs. Consensus amongst multidisciplinary clinical and academic experts accompanies these reviews. Theoretically, consensus indicates that guidelines would accelerate dissemination and incorporation of the most up-to-date scientific evidence into everyday clinical practice [Reference Forsner, Hansson, Brommels, Wistedt and Forsell20]. This in turn could reduce inappropriate practice variation [Reference Kung, Miller and Mackowiak21] and improve coordination of care across involved agencies and choice of efficacious interventions. However, concerns have also been expressed that guidelines provide an oversimplified “cook book” approach to address complex clinical questions . Additionally, they may restrict clinicians’ autonomy in customising interventions to individual patients, local resources, or cultural values [Reference Forsner, Hansson, Brommels, Wistedt and Forsell20, Reference Scott and Guyatt22]. The question that arises is whether such clinical guidelines for children with SBPs are available across different European countries and, when available, whether they are perceived as fit-for-purpose.
This study aimed to compile a preliminary summary of European academic experts’ reflections on the availability, contribution of and need for developing guidelines for the diagnostics and treatment of SBPs in children. Knowledge on additional unofficial documents on SBPs, such as textbooks, publications, or intervention manuals was also collected. In Europe, many experts are involved in guidelines planning and evaluation (e.g., [Reference Wolf, Hubbard, Faraday and Forrest23]). Collecting experts’ opinions would provide the beginning of further systematically conducted, in-depth analyses of guidelines implementation between and within countries, and help identify current facilitators and barriers to implementing evidence into practice to proffer educated solutions.
2.1. Recruitment and participants
The Knowledge Centre of Child and Adolescent Psychiatry in The Netherlands was first approached to locate experts in SBPs within the Netherlands. Moreover, the authors (A.R.G., A.L., L.vD., and R.V.) screened for members of European child and adolescent mental health organisations, such as the European Society of Child and Adolescent Psychiatry, the European Association for Forensic Child & Adolescent Psychiatry, Psychology & other Involved Professions, and Consortium Aggression in Children: Unravelling gene-environment interplay to inform Treatment and InterventiON strategies (ACTION). Lastly, the authors screened peer-reviewed scientific publications on ODD or CD for recurrent authors. These publications were retrieved based on search terms such as: “childhood aggression”, “disruptive behaviour disorders”, or “conduct disorder” on PsycInfo, Medline and Embase platforms and evidence-based programs websites such as Incredible Years [Reference Webster-Stratton and Reid24] and Triple P [Reference Sanders25]. Given that no exhaustive list of experts in SBPs was available, screening literature and case snowball sampling were used based on previous Delphi expert panel studies [Reference Mittnacht and Bulik26–Reference Kloser29].
Expertise was also established based on previously employed criteria [e.g., conference presentations, articles/ books authorships; [Reference Sanders25–Reference Ross, Kelly and Jorm28]. Therefore, at screening stage, potential experts were included if they met either of the minimum criteria: lead authorship of national/international publications on SBPs; research on or involvement in evidence-based programs for SBPs; participation in guidelines development for SBPs; or recommendation from academic colleagues. This was followed by further investigation of potential experts’ research profiles on institutional/ professional websites, publication history and involvement in national bodies, all of which had to target SBPs as a primary field. Corroborating these criteria led to an estimate of one’s expertise. To account for financial and language barriers that may have prevented experts from lower developed countries to be identified, such experts were invited if at least one of the criteria above was met. Once invited, all experts were able to express whether they felt sufficiently knowledgeable to participate or recommended a suitable colleague. Altogether, 72 experts from 28 European countries were invited. Responses were received from 28 experts (38.9%) representing 23 countries, with both medical (50%) and psychology (50%) educational backgrounds and an array of professional roles and experiences. This diversity in the expert group has been deemed valuable in similar expert panel studies [Reference Jorm27]. Of the 44 experts that did not provide answers, seven felt unsuitable to participate and recommended colleagues. Respondents’ and non-respondents’ professional roles are presented in Tables 1–2.
Note. Some academics have more than one title and have been endorsed under all relevant categories.. Titles and positions have been retrieved through online manual searches and may not be exhaustive of experts’ current roles. Percentages were calculated out of the total number of experts, N = 28.
Note. Some academics have more than one title and have been endorsed under all relevant categories. Titles and positions have been retrieved through online manual searches and may not be exhaustive of experts’ current roles. Percentages were calculated out of the total number of non-respondent experts, n = 44.
An electronic semi-structured questionnaire was developed for this study. The questionnaire included a definition of SBPs and 12 questions. SBPs in childhood (6–12 years old), placed at the severe end of the behavioural disorders continuum, were defined as persistent and frequent oppositional, aggressive, and destructive behaviours, occurring across settings, and interfering with daily functioning. This definition was formulated by the authors (A.L., A.R.G, L.vD., and R.V.) based on descriptions of ODD, CD, and disruptive behaviour disorders in childhood in the literature (e.g. [Reference Matthys6, Reference Lahey and Waldman9]). The questionnaire was compiled by A.L. and A.R.G., with feedback from three other authors (M.C., L.vD., and R.V.), and reviews from three experts in qualitative research. The questionnaire was piloted on five experts from different European countries. Their responses reflected good understanding of the questions, indicating that the questionnaire explored what it was intended to. The first topic covered explored the availability, utility, and critical needs of official guidelines and/or unofficial documents for diagnosing and treating SBPs in children. The second topic covered the need for developing such national and/or European guidelines. The questionnaire is available upon request.
Responses were collected on the online platform Qualtrics. Experts were invited to participate via a personalised email, followed by three weekly email reminders, and a final reminder sent via the person who recommended the expert, where available. Lastly, a member check was conducted, in which experts checked whether their opinion/country was correctly represented in a written report summarising the answers. This quality control process was performed to ensure that responses were accurately analysed [cf.,Reference Harper and Cole30], and that experts’ answers in each country were accurately represented. Of the 28 experts, 22 provided feedback on the report within a two-week timeframe. All minor corrections resulting from the member check were carried out and the final outcomes are further reported. The data collection process was guided by a Delphi procedure [Reference Jorm27], although it differed from a Delphi study by being explorative rather than seeking to establish consensus. Data collection was conducted over a period of eight months.
2.4. Data analysis
Definitions of guidelines/ documents were developed following data collection. Official clinical guidelines included a systematic, evidence-based set of recommendations for the diagnostics and treatment of SBPs in children, that were created following collective efforts from academic experts, clinicians, and relevant institutions. Unofficial clinical documents were regarded as textbooks, chapters, publications, intervention manuals, or practice parameters on externalising disorders, containing guidance on either diagnostics or treatment or both for SBPs in children. The authors used these definitions to categorise the documents mentioned by experts into the corresponding group. For broader open-ended questions, extraction of themes was done in line with thematic analysis steps. These involved familiarization with the data, generating initial codes, and identifying, reviewing, and defining themes [Reference Maguire and Delahunt31, Reference Braun and Clarke32]. Due to the very brief answers offered by experts, the analysis was limited to identifying semantic, surface meanings, rather than rich latent-level conceptualisations [Reference Braun and Clarke32]. To organise information into multilevel lists, numerical codes were annexed to themes and sub-themes, in line with previous studies [Reference Mittnacht and Bulik26, Reference Huijg, Gebhardt, Crone, Dusseldorp and Presseau33]. For instance, Huijg et al. [Reference Huijg, Gebhardt, Crone, Dusseldorp and Presseau33] coded the domain ‘Emotion’ as ‘D13’ out of the 14 domains studied, under which two subordinate constructs were coded: Affect, and Stress. Similarly, we coded themes such as ‘familiarity with guidelines’ as ‘1’, with sub-themes as: ‘1.1. little familiarity’, ‘1.2. average familiarity’, and ‘1.3. good familiarity’. Two authors have independently reviewed and coded 25% of the data (A.L., and A.R.G.). A 95% agreement was achieved for the highest-level broader codes/themes in the open-ended questions (e.g., professionals using guidelines), and categorical questions (e.g., ‘are guidelines available?’). Divergences emerging at sub-themes levels were fully resolved by reviewing the constructs through a telephone meeting. All responses were exhaustively represented under the final themes. Frequencies with which a theme/sub-theme was mentioned were also reported. To assess for saturation of data, we used the inductive thematic approach by which saturation occurred when no novel codes/themes emerged in data analysis [Reference Birks and Mills34, Reference Saunders, Sim, Kingstone, Baker, Waterfield and Bartlam35]. Data closely approached thematic saturation on discussing the need for developing, or utility and critical needs for guidelines. Lack of saturation on questions such as the utility and critical needs for unofficial documents may have reflected an artefact of the great variety in unofficial documents referred to by clinicians. Overall, adding that previous Delphi studies using expert panels also identified that data gets saturated in expert panels that exceed thirty participants, number which we nearly reached [Reference Kloser29], we were confident that some of our material reached saturation.
3.1. Official clinical guidelines
According to experts’ knowledge (N = 28 from 23 countries), 10 out of 23 countries possessed official guidelines for SBPs in children (43.5%), and Finland intended to publish national guidelines for conduct disorder in December 2018 (Fig.1). Most guidelines were developed by a group of experts within the national public health services/directorate or national child psychiatry associations. Overall, child psychiatrists were the professionals most frequently mentioned as drawing on these official clinical guidelines to inform practices across Europe (n = 7 countries), followed by psychologists (n = 6 countries), teachers (n = 4 countries), social services (n = 2 countries) and paediatricians (n = 1 country). Professionals’ familiarity with guidelines ranged from guidelines being generally ignored, to “almost all (those employed in the official mental health service) being familiar with these (guidelines) and should abide them.” (expert opinion).
3.1.2. Utility and critical needs
The content of clinical guidelines was perceived as helpful in daily practice by experts in six out of the ten countries currently having such guidelines: “It is a good reference for everyday work. The professional feels safer because s/he knows what do to for each disorder with guarantee of choosing a good intervention (evidence-based).” However, experts identified the following critical needs that should be addressed to improve existing guidelines. Content related adjustments included adding specific recommendations for individual case management, including recommendations for severely aggressive patients (e.g., de-escalation strategies in hospitals) (n = 2) and incorporating forensic perspectives such as offence orientated psychotherapy (n = 2). Implementation efforts consisted of collecting feedback from practitioners to better tailor recommendations to clinical practice (n = 1), persuading commissioners to prioritise SBPs (n = 1), and training staff in recommended evidence-based methods (EBMs), including parent training and cognitive behavioural therapy-based programs (n = 1).
3.2. Unofficial clinical documents
Experts in 14 out of the 23 countries indicated that unofficial clinical documents were available (60.9%). In seven of these countries these unofficial documents were used alongside official guidelines (Fig. 1). These included clinical reports, manuals or psychiatry textbooks on ODD/CD in children (n = 12), national and/or international practice parameters for CD (n = 1), and governmental sponsored recommendations respectively (e.g., The Incredible Years, [Reference Webster-Stratton and Reid24] etc.; n = 1). According to the experts’ knowledge, psychiatrists (n = 13 countries) and psychologists (n = 12 countries) were the professionals who used these documents most actively across Europe, followed by teachers (n = 2 countries), social/child protection services (n = 2 countries), psychotherapists (n = 2 countries), and general practitioners (n = 1 country). Their familiarity with these documents varied from little (e.g., ‘Far from all know about them and use them. I Think many need more training to be able to apply them.’) to good familiarity across countries (e.g., ‘These official, but not mandatory, suggestions are widely followed by psychiatrists, psychologists and social workers alike’) based on experts’ views.
3.2.2. Utility and critical needs
Unofficial clinical documents were perceived as helpful in guiding clinical practice by experts in three countries. On the one hand, maximising the practical value of these documents were content components such as EBM recommendations (n = 1) and/or behavioural management models (n = 1), and implementation aspects such as support from (governmental) health authorities via staff training (n = 1), or offering a wide range of treatment recommendations and approaches to support personalising interventions (n = 1). On the other hand, experts identified several problems underlying the content and use of such documents in clinical practice. At content level, they lacked cohesiveness and breadth of approaches (n = 4) or evidence-based interventions (n = 1). Implementation challenges included limitations over the resources for assessment and treatment (n = 2) and translated resources (n = 1) available in practice to apply documents recommendations, inconsistent application of tools between practitioners (n = 2), practitioners’ limited knowledge about existing recommendations (n = 1), and the format of such documents being hard to translate in practice (n = 1). Critical needs included developing a clear, specific, and practical clinical guideline for SBPs (n = 7) accompanied by a dissemination program (n = 1), improving measures for existing EBM resources and more randomized-control trials on medication effectiveness (n = 1).
3.3. Need for national and/or european clinical guidelines for SBPs
Of the experts reporting on whether national guidelines for SBPs in children are needed (n = 27 from 22 countries), at least one expert was in favour of developing such guidelines in 16 countries (n = 18, 66.7%). Of the experts reporting on whether European guidelines for SBPs in children are needed (n = 25 from 21 countries), at least one expert was in favour of developing such guidelines in 19 countries (n = 21, 84%). Themes emerging on the benefits and drawbacks of developing such guidelines are presented in Table 3.
This study provides a first insight into the availability and utility of clinical guidelines for SBPs in children across Europe, based on academic experts’ knowledge. Experts indicated that official guidelines and unofficial documents were available in nearly half and two thirds of countries respectively. Two key lessons offered by experts are highlighted. First, official clinical guidelines for SBPs are regarded as beneficial, but their implementation needs to be reinforced and content better tailored to daily practice. Second, having a diverse pool of recommendations is beneficial in individualising treatment. However, attention is directed towards a better standardisation of practices, through the collaborative creation of national and/or European clinical guidelines for SBPs.
First, our findings indicate that guidelines provide support for evidence-based clinical decisions. A salient challenge is clinicians familiarising with and implementing them in practice. This issue reflects previous warnings that guidelines need to be accompanied by implementation tools such as instructions on overcoming barriers for their use in practice to be maximised [Reference Gagliardi and Brouwers36, Reference Pronovost37]. Experts offered suggestions for improvement, including the incorporation of specific recommendations to reflect the diversity of cases in daily practice, training staff to increase familiarity with guidelines and EBMs implicitly, and persuading commissioners to prioritise SBPs. These mirror at a larger scale, critical needs in public mental health initiatives. For instance, a systematic meta-review identified that including recommendations for complex presentations within guidelines might facilitate translating population-based guidelines into individualized formulations and treatment plans [Reference Francke, Smit, de Veer and Mistiaen4], see also [Reference Carr16]. Additionally, insufficient training usually results in poor familiarity with guidelines [Reference Winther, Carlsson and Vance38], a factor consistently mentioned as a barrier to implementation [Reference Joshi39–Reference Schoenwald, Kelleher, Weisz, Chorpita, Gibbons and Glisson41]. Finally, senior government decision-makers on mental health, public health experts and academics internationally have stressed that mental health care deserves more attention [Reference Saraceno, van Ommeren, Batniji, Cohen, Gureje and Mahoney42], an aspect also highlighted with regards to SBPs by experts in this study.
The second lesson taught by experts is that a shift towards a comprehensive, shared pool of recommendations is needed to reduce the unwarranted practice variation that may arise with the use of unofficial clinical documents exclusively. The development of official national/ European clinical guidelines would answer this plea. 66.7% and 84% experts respectively called for the development and dissemination of national and European guidelines on SBPs in children, mirroring professional consensus on the topic in other fields  and recent developments of European guidelines for other paediatric mental health disorders [Reference Taylor, Döpfner and Sergeant44]. National and European guidelines share three main benefits according to experts’ opinions. They would encourage standardised clinical decision-making, create a shared understanding of SBPs for researchers and clinicians, and increase accessibility to EBMs and early intervention. These would address previous calls for increasing awareness of SBPs and early intervention [Reference Burke and Loeber45]. However, experts emphasised the potentially superior value of European guidelines, although acknowledging the challenges social, health, and cultural differences between countries create. European guidelines were believed to support the development of a national guideline, answering calls for globalising the evidence while localising the recommendations [Reference Eisenberg46]. Additionally, they could maximise harmony between clinical practices and stimulate negotiations amongst multi-disciplinary professionals both within and between countries [Reference Koivusalo, Labonte, Wibulpolprasert, Kancahanchitra, Leppo, Ollila, Pena, Wismar and Cook5].
Nevertheless, the study had several significant limitations. First, there was selection bias, as case snowball sampling and screening of literature primarily written in English were used. Despite being the best available and commonly employed method in this type of research [Reference Mittnacht and Bulik26, Reference Ross, Kelly and Jorm28, Reference Kloser29], this may have increased heterogeneity in experts’ levels of knowledge and dismissed potentially suitable experts. Thus, the results present only preliminary subjective opinions, rather than a comprehensive objective inventory on guidelines across countries. These could inform future systematic or qualitative studies investigating information derived from a range of stakeholders sampled in a more systematic manner, such as practitioners rating their use of guidelines and perceptions of usefulness and need for change. Second, SBPs associated with other disorders (ie. ADHD, ASD, learning disability etc.) were not specifically excluded from the definition. Therefore, recommendations on SBPs management may have also been available in clinical guidelines for comorbid conditions or neurodevelopmental disorders, potentially increasing inconsistencies between what documents respondents reported about. Finally, we have not checked whether experts used high quality systematic evidence such as audits, governmental reports, or meta-analyses, or personal/ professional experience to inform judgments on guidelines, concerns highlighted in previous Delphi studies [e.g., 27]. This poses threats over the degree of accuracy and generalisability of the data. Future researchers should thus explicitly identify experts’ data sources in the answers, or collect such reports themselves, using experts as facilitators in identifying the reports in the first place.
Overall, based on this study’s findings, guidelines better adjusted to clinical practice should include a wide pool of EBMs, specific recommendations for different presentations (e.g., de-escalation strategies for severely aggressive patients), and feedback from practitioners. Implementation efforts could encompass persuading commissioners to prioritise SBPs, training staff in recommended EBMs, securing national government/ health authorities support, formatting guidelines in a clinically-friendly, concise and clear way, translating recommendations, and providing adjacent dissemination instructions. Finally, the high comorbidity between SBPs and other neurodevelopmental or mental health disorders [Reference Pijper, de Wied, van Rijn, van Goozen, Swaab and Meeus47–Reference Connor, Steeber and McBurnett49] stresses the importance of aligning SBP guidelines with guidelines for other overlapping disorders.
The present study has research, service and policy implications. First, experts stressed that guidelines would enhance clarity between research and clinical practice on SBPs. Second, implementation of guidelines should be improved. Third, having a consensus-based national or European framework for managing SBPs in children would strengthen incorporation of evidence in clinical-decision making, increase awareness, and thus early intervention for this group. This study instils a momentum for the creation of European clinical guidelines for this population.
Declarations of interest
The manuscript does not contain clinical studies or patient data. Declarations of interest: None.
Key experts in the field of SBPs in Europe who completed the questionnaire included: P.D. Dr. Belinda Plattner (Austria), Prof. Dr. Dirk van West (Belgium), Assoc. Prof. Kostas Fanti (Cyprus), Prof. Dr. Eeva Aronen (Finland), Prof. Dr. David Cohen (France), Prof. Dr. Christine Freitag (Germany), Prof. Dr. Christina Stadler (Germany), Assoc. Prof. Dr. Dimitris Anagnostopoulos (Greece), Dr.Margrét Sigmarsdóttir (Iceland), Dr. Pietro Muratori (Italy), Dr. Darius Leskaukas (Lithuania), Dr. Roland Paulauskas (Lithuania), Assoc. Prof. Jana Chihai (Repulic of Moldova), Prof. Emerit. Walter Matthys (Netherlands), Prof. Dr. Terje Ogden (Norway), Prof. Dr. Lars Wichstrom (Norway), Prof. Dr. Daniel Rijo (Portugal), Prof. Dr. Ricardo Barroso (Portugal), Assist. Prof. Dr. Elena Predescu (Romania), Assist. Prof. Maja Drobnic Radobuljac (Slovenia), Prof. Dr. Stephen Scott (UK). Experts in four countries wished not to be mentioned in publications resulting from this project. Experts in a remaining three countries did not indicate whether they wish to be mentioned. Additionally, experts in qualitative research and psychiatric research ethics who contributed to the creation, revision and analysis of the questionnaire included: Dr. Matty Crone, Prof. Dr. Catrin Finkenauer, Prof. Dr. Gerben Meynen, Prof. Dr. Ria Reis, Jeroen de Winter (Clin. Psy.), and Anne Hendriks (PhD Candidate). work was supported by ACTION (Aggression in Children: unravelling gene-environment interplay to inform Treatment and InterventiON strategies), funded under the European Union Seventh Framework Program (FP7/2007-2013) [grant number 602768].
Appendix A. List of guidelines and unofficial documents referred to by experts
Note. ‘Not reported’ indicates that the expert did not provide an answer. Information in the tables has been presented as reported by experts.
Appendix B. Authors details
Alexandra-Raluca Gatej started working as a student research assistant at Curium-LUMC, Centre for Child and Youth Psychiatry in November 2015. She completed the MSc Child & Adolescent Psychology program, at Leiden University in August 2016, and has since been continuing her collaboration with Curium-LUMC as a PhD student through a part-time route. She is also currently completing the MSc in Applied Psychology for Children and Young People at University of Edinburgh, Scotland, working within a Child and Adolescent Mental Health Service in Glasgow, United Kingdom.
Audri Lamers is a qualified clinical psychologist and senior researcher. In 2016, she successfully defended her PhD thesis on the parent-team therapeutic alliance in child psychiatry. During the development of this project, Audri worked as a clinical psychologist and senior researcher at Curium-LUMC. Currently she works in De Opvoedpoli Child and Youth Psychiatry and continues combining clinical work and scientific research with a special interest in the application of scientific research results to improve the quality of clinical work.
Lieke van Domburgh is director of quality of care and innovation at Pluryn-Intermetzo, a multi-site center for multiproblem youth and adults both with and without co-morbid mental and physical disabilities, and senior researcher in child and adolescent psychiatry at VU University Medical Center Amsterdam (VUMC). She obtained her doctorate on the development of children under 12 who have been in contact with the police. Her expertise lies within the field of children and young people with serious behavioural problems in (judicial) youth care and cultural diversity.
Matty Crone is an associate professor within the prevention and community care field at the department of public health and community care, Leiden University Medical Center (LUMC). She has extensive research experience in the field of youth and is involved in various studies on the prevention of unhealthy lifestyles amongst young people and the identification of psychosocial problems by Youth Health Care and general practitioners.
Terje Ogden is professor at the department of psychology, University of Oslo, research director at the Centre for Studies of Behavioural Problems and Innovative Practice, The Centre for Behavioural Research – Unirand, and director of research at the Norwegian Centre for Child Behavioural Development. His research expertise lies within the domain of children behavioural problems, positive behaviour in schools and parent training programs. He is editor in several international journals, including Journal of Emotional and Behavioural Difficulties and Journal of Prevention Science.
Daniel Rijo is associate professor at the Cognitive and Behavioral Centre for Research and Intervention and Faculty of Psychology and Education Sciences, University of Coimbra, Portugal. He obtained his doctorate in clinical psychology at the University of Coimbra. Daniel published numerous scientific articles, books and chapters on topics such as psychopathy, antisocial behaviour, and mental health services in legal institutions.
Eeva Aronen is a qualified child psychiatrist, MD, PhD, and professor of child psychiatry at Helsinki University. Her affiliations are at Helsinki University, Helsinki University Hospital, and Helsinki Pediatric Research Center, Laboratory of Developmental Psychopathology. The main focus of Eeva's scientific research is on sleep and executive functions in children, the protective and risk factors affecting a child's development, behavioral disorders in children and their treatment.
Ricardo Barroso is a qualified clinical and forensic psychologist, and PhD. He works as an assistant professor at the University of Trás-os-Montes and Alto Douro (Portugal), and senior researcher at the research laboratory in human sexuality (SexLab), University of Porto, which focuses on sexual aggression and atypical interests. Ricardo is also offering consultancy in various national and international governmental organizations and has been a member of the Board of the European Association for Forensic Child & Adolescent Psychiatry and Psychology (EFCAP).
Dorret I. Boomsma is a professor in the department of biological psychology, VU University Amsterdam, and a leading scientist in twin and genetic studies of behavior, health and psychopathology. Dorret has numerous scientific publications on topics such as ADHD in children and behavioural problems in children, with a focus on epigenetics. She is also the coordinator of the ACTION consortium on pediatric aggression, which this project is branching from.
Robert Vermeiren is a qualified child and adolescent psychiatrist. He currently works as a professor of child and adolescent psychiatry at Leiden University Medical Centre, director of patient care of the child psychiatric clinic Curium-LUMC and head of research in De Jutters- Lucertis Parnassia Group for child and adolescent psychiatry. He is also professor of forensic child and youth psychiatry at the VU University Medical Center Amsterdam. Within the ACTION consortium, Robert is the leader of this project.
CommentsNo Comments have been published for this article.